Solid polymer electrolytes based on polystyrene‐polyether block copolymers having branched ether structure
To obtain solid polymer electrolytes (SPEs) having high ionic conductivity together with mechanical integrity, we have synthesized polystyrene (PSt)‐polyether (PE) diblock copolymers via one‐pot anionic polymerization. The PSt block is expected to aggregate to act as hard fillers in the SPE to enhan...
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Veröffentlicht in: | Polymers for advanced technologies 2019-03, Vol.30 (3), p.736-742 |
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description | To obtain solid polymer electrolytes (SPEs) having high ionic conductivity together with mechanical integrity, we have synthesized polystyrene (PSt)‐polyether (PE) diblock copolymers via one‐pot anionic polymerization. The PSt block is expected to aggregate to act as hard fillers in the SPE to enhance the mechanical property. The PE block consists of random copolymer (P(EO‐r‐MEEGE)) of ethylene oxide (EO) and 2‐(2‐methoxyethoxy) ethyl glycidyl ether (MEEGE) in different molar ratios ([EO]/[MEEGE] = 100/0, 86/14, 75/25, 68/32, and 41/59). The introduction of the MEEGE moiety in PEO reduced the crystallinity of PEO, and the fast motion of the MEEGE side chain caused plasticization of the PE block, thereby contributing to the fast ion transport. SPEs were fabricated by mixing the obtained diblock copolymer (PSEx) and lithium bis(trifluoromethanesulfonyl) amide (LiTFSA) with [Li]/[O] = 0.05. Ionic conductivity of the obtained SPEs was dependent on the molar ratio of EO in the PE block (x) as well as the weight fraction of PE block (fPE) in the block copolymer. PSE0.86 (fPE = 0.65) exhibited high ionic conductivity (3.3 × 10−5 S cm−1 at 30°C; 1.1 × 10−4 S cm−1 at 60°C) comparable with that of P(EO‐r‐MEEGE) (PE0.85; fPE = 1.00) (9.8 × 10−5 S cm−1 at 30°C; 4.0 × 10−4 S cm−1 at 60°C). |
doi_str_mv | 10.1002/pat.4511 |
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The PSt block is expected to aggregate to act as hard fillers in the SPE to enhance the mechanical property. The PE block consists of random copolymer (P(EO‐r‐MEEGE)) of ethylene oxide (EO) and 2‐(2‐methoxyethoxy) ethyl glycidyl ether (MEEGE) in different molar ratios ([EO]/[MEEGE] = 100/0, 86/14, 75/25, 68/32, and 41/59). The introduction of the MEEGE moiety in PEO reduced the crystallinity of PEO, and the fast motion of the MEEGE side chain caused plasticization of the PE block, thereby contributing to the fast ion transport. SPEs were fabricated by mixing the obtained diblock copolymer (PSEx) and lithium bis(trifluoromethanesulfonyl) amide (LiTFSA) with [Li]/[O] = 0.05. Ionic conductivity of the obtained SPEs was dependent on the molar ratio of EO in the PE block (x) as well as the weight fraction of PE block (fPE) in the block copolymer. PSE0.86 (fPE = 0.65) exhibited high ionic conductivity (3.3 × 10−5 S cm−1 at 30°C; 1.1 × 10−4 S cm−1 at 60°C) comparable with that of P(EO‐r‐MEEGE) (PE0.85; fPE = 1.00) (9.8 × 10−5 S cm−1 at 30°C; 4.0 × 10−4 S cm−1 at 60°C).</description><identifier>ISSN: 1042-7147</identifier><identifier>EISSN: 1099-1581</identifier><identifier>DOI: 10.1002/pat.4511</identifier><language>eng</language><publisher>Bognor Regis: Wiley Subscription Services, Inc</publisher><subject>Anionic polymerization ; block copolymer ; Block copolymers ; Chemical synthesis ; Electrolytes ; Ethylene oxide ; Fillers ; Ion currents ; Ion transport ; Ions ; Lithium ; Molten salt electrolytes ; one‐pot living anionic polymerization ; Polyethylenes ; Polystyrene resins ; Solid electrolytes ; solid polymer electrolytes ; Weight</subject><ispartof>Polymers for advanced technologies, 2019-03, Vol.30 (3), p.736-742</ispartof><rights>2018 John Wiley & Sons, Ltd.</rights><rights>2019 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4401-bf5efaaafdaa3f6af6039bed0a3d55c772051760dc1f915d096358339f9466703</citedby><cites>FETCH-LOGICAL-c4401-bf5efaaafdaa3f6af6039bed0a3d55c772051760dc1f915d096358339f9466703</cites><orcidid>0000-0003-4092-6150 ; 0000-0001-9994-2863</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpat.4511$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpat.4511$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Kokubo, Hisashi</creatorcontrib><creatorcontrib>Nakazawa, Eiji</creatorcontrib><creatorcontrib>Watanabe, Masayoshi</creatorcontrib><title>Solid polymer electrolytes based on polystyrene‐polyether block copolymers having branched ether structure</title><title>Polymers for advanced technologies</title><description>To obtain solid polymer electrolytes (SPEs) having high ionic conductivity together with mechanical integrity, we have synthesized polystyrene (PSt)‐polyether (PE) diblock copolymers via one‐pot anionic polymerization. The PSt block is expected to aggregate to act as hard fillers in the SPE to enhance the mechanical property. The PE block consists of random copolymer (P(EO‐r‐MEEGE)) of ethylene oxide (EO) and 2‐(2‐methoxyethoxy) ethyl glycidyl ether (MEEGE) in different molar ratios ([EO]/[MEEGE] = 100/0, 86/14, 75/25, 68/32, and 41/59). The introduction of the MEEGE moiety in PEO reduced the crystallinity of PEO, and the fast motion of the MEEGE side chain caused plasticization of the PE block, thereby contributing to the fast ion transport. SPEs were fabricated by mixing the obtained diblock copolymer (PSEx) and lithium bis(trifluoromethanesulfonyl) amide (LiTFSA) with [Li]/[O] = 0.05. Ionic conductivity of the obtained SPEs was dependent on the molar ratio of EO in the PE block (x) as well as the weight fraction of PE block (fPE) in the block copolymer. PSE0.86 (fPE = 0.65) exhibited high ionic conductivity (3.3 × 10−5 S cm−1 at 30°C; 1.1 × 10−4 S cm−1 at 60°C) comparable with that of P(EO‐r‐MEEGE) (PE0.85; fPE = 1.00) (9.8 × 10−5 S cm−1 at 30°C; 4.0 × 10−4 S cm−1 at 60°C).</description><subject>Anionic polymerization</subject><subject>block copolymer</subject><subject>Block copolymers</subject><subject>Chemical synthesis</subject><subject>Electrolytes</subject><subject>Ethylene oxide</subject><subject>Fillers</subject><subject>Ion currents</subject><subject>Ion transport</subject><subject>Ions</subject><subject>Lithium</subject><subject>Molten salt electrolytes</subject><subject>one‐pot living anionic polymerization</subject><subject>Polyethylenes</subject><subject>Polystyrene resins</subject><subject>Solid electrolytes</subject><subject>solid polymer electrolytes</subject><subject>Weight</subject><issn>1042-7147</issn><issn>1099-1581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp10M1KxDAQB_AgCq6r4CMUvHjpmmmbZnNcFr9gQcH1HNI0cbt2m5qkSm8-gs_ok5hu9-ppMsxvJvBH6BLwDDBOblrhZxkBOEITwIzFQOZwPLyzJKaQ0VN05twW4zBjdILqF1NXZdSaut8pG6laSW9D45WLCuFUGZlmP3W-t6pRv98_Q6f8JuiiNvI9kuaw7aKN-Kyat6iwopGbsDsy520nfWfVOTrRonbq4lCn6PXudr18iFdP94_LxSqWWYYhLjRRWgihSyFSnQud45QVqsQiLQmRlCaYAM1xKUEzICVmeUrmaco0y_Kc4nSKrsa7rTUfnXKeb01nm_AlT4AGAHNGgroelbTGOas0b221E7bngPmQJQ9Z8iHLQOORflW16v91_Hmx3vs_u8V46A</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Kokubo, Hisashi</creator><creator>Nakazawa, Eiji</creator><creator>Watanabe, Masayoshi</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0003-4092-6150</orcidid><orcidid>https://orcid.org/0000-0001-9994-2863</orcidid></search><sort><creationdate>201903</creationdate><title>Solid polymer electrolytes based on polystyrene‐polyether block copolymers having branched ether structure</title><author>Kokubo, Hisashi ; Nakazawa, Eiji ; Watanabe, Masayoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4401-bf5efaaafdaa3f6af6039bed0a3d55c772051760dc1f915d096358339f9466703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anionic polymerization</topic><topic>block copolymer</topic><topic>Block copolymers</topic><topic>Chemical synthesis</topic><topic>Electrolytes</topic><topic>Ethylene oxide</topic><topic>Fillers</topic><topic>Ion currents</topic><topic>Ion transport</topic><topic>Ions</topic><topic>Lithium</topic><topic>Molten salt electrolytes</topic><topic>one‐pot living anionic polymerization</topic><topic>Polyethylenes</topic><topic>Polystyrene resins</topic><topic>Solid electrolytes</topic><topic>solid polymer electrolytes</topic><topic>Weight</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kokubo, Hisashi</creatorcontrib><creatorcontrib>Nakazawa, Eiji</creatorcontrib><creatorcontrib>Watanabe, Masayoshi</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymers for advanced technologies</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kokubo, Hisashi</au><au>Nakazawa, Eiji</au><au>Watanabe, Masayoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Solid polymer electrolytes based on polystyrene‐polyether block copolymers having branched ether structure</atitle><jtitle>Polymers for advanced technologies</jtitle><date>2019-03</date><risdate>2019</risdate><volume>30</volume><issue>3</issue><spage>736</spage><epage>742</epage><pages>736-742</pages><issn>1042-7147</issn><eissn>1099-1581</eissn><abstract>To obtain solid polymer electrolytes (SPEs) having high ionic conductivity together with mechanical integrity, we have synthesized polystyrene (PSt)‐polyether (PE) diblock copolymers via one‐pot anionic polymerization. The PSt block is expected to aggregate to act as hard fillers in the SPE to enhance the mechanical property. The PE block consists of random copolymer (P(EO‐r‐MEEGE)) of ethylene oxide (EO) and 2‐(2‐methoxyethoxy) ethyl glycidyl ether (MEEGE) in different molar ratios ([EO]/[MEEGE] = 100/0, 86/14, 75/25, 68/32, and 41/59). The introduction of the MEEGE moiety in PEO reduced the crystallinity of PEO, and the fast motion of the MEEGE side chain caused plasticization of the PE block, thereby contributing to the fast ion transport. SPEs were fabricated by mixing the obtained diblock copolymer (PSEx) and lithium bis(trifluoromethanesulfonyl) amide (LiTFSA) with [Li]/[O] = 0.05. Ionic conductivity of the obtained SPEs was dependent on the molar ratio of EO in the PE block (x) as well as the weight fraction of PE block (fPE) in the block copolymer. PSE0.86 (fPE = 0.65) exhibited high ionic conductivity (3.3 × 10−5 S cm−1 at 30°C; 1.1 × 10−4 S cm−1 at 60°C) comparable with that of P(EO‐r‐MEEGE) (PE0.85; fPE = 1.00) (9.8 × 10−5 S cm−1 at 30°C; 4.0 × 10−4 S cm−1 at 60°C).</abstract><cop>Bognor Regis</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/pat.4511</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-4092-6150</orcidid><orcidid>https://orcid.org/0000-0001-9994-2863</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anionic polymerization block copolymer Block copolymers Chemical synthesis Electrolytes Ethylene oxide Fillers Ion currents Ion transport Ions Lithium Molten salt electrolytes one‐pot living anionic polymerization Polyethylenes Polystyrene resins Solid electrolytes solid polymer electrolytes Weight |
title | Solid polymer electrolytes based on polystyrene‐polyether block copolymers having branched ether structure |
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